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rs1064793889

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome9
Position127818780
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1064793889
dbSNP (old)rs1064793889
ClinGenrs1064793889
ebirs1064793889
HLIrs1064793889
Exacrs1064793889
Gnomadrs1064793889
Varsomers1064793889
Maprs1064793889
PheGenIrs1064793889
Biobankrs1064793889
1000 genomesrs1064793889
hgdprs1064793889
ensemblrs1064793889
gopubmedrs1064793889
geneviewrs1064793889
scholarrs1064793889
googlers1064793889
pharmgkbrs1064793889
gwascentralrs1064793889
openSNPrs1064793889
23andMers1064793889
23andMe allrs1064793889
SNPshotrs1064793889
SNPdbers1064793889
MSV3drs1064793889
GWAS Ctlgrs1064793889
Max Magnitude0
ClinVar
Risk rs1064793889(C;C)
Alt rs1064793889(C;C)
Reference Rs1064793889(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG LOC102723566
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130581059_130581060insG
CLNSRC
CLNACC RCV000482568.1,